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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to November 2026.

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls

Most common hazardLack of Assurance of Sterility 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 9, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: February 28, 2018Historical recordClass III

Mefenamic Acid, 250mg capsules, packaged in 30-count bottles, Rx Only, Distributed by: Prasco Laboratories Mason, OH 45040 USA, Manufactured by: Halo Pharmaceutical Inc. Whippany, NJ 07981, NDC 66993-070-30

by Shionogi Inc.

Reason: Failed Dissolution Specifications: Low dissolution results were obtained during stability testing
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 10, 2019Historical recordClass III

Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 5 mL Single-use vial, Rx Only, Sterile, Manufactured by: Gland Pharma Limited, Hyderabad, India, Manufactured for: Hospira, Inc, Lake Forest, IL 60045 --- NDC 0409-1140-01

by Hospira Inc., A Pfizer Company

Reason: Failed Impurities/Degradation Specifications; out of specification result for denitroquinoline-related impurity during three month time point
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B99187, BREADER X1, NET WT 50 LBS, Manufactured By: Newly We…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B94797, BREADER X1@, NET WT 40 LBS, Manufactured By: Newly W…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B94412, BREADER X1@, NET WT 50 LBS, Manufactured By: Newly W…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B94128, BREADER X1, NET WT 50 LBS, Manufactured By: Newly We…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B94110, BREADER X1, NET WT 50 LBS, Manufactured By: Newly We…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B94109, BREADER X1@, NET WT 50 LBS, Manufactured By: Newly W…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B93836, BREADER X1, NET WT 25 LBS, Manufactured By: Newly We…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B93709, BREADER X1@, NET WT 40 LBS, Manufactured By: Newly W…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B93706, BREADER X5, NET WT 50 LBS, Manufactured By: Newly We…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B92659, BREADER X1@, NET WT 35 LBS, Manufactured By: Newly W…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B89414, BATTER MX X1@, NET WT 50 LBS, Manufactured By: Newly…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B89223, BATTER MX X1@, NET WT 50 LBS, Manufactured By: Newly…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B88991, BATTER MX X1@, NET WT 20 LBS, Manufactured By: Newly…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B86031, BATTER MX X1*, NET WT 50 LBS, Manufactured By: Newly…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B84127, BATTER MIX X1, NET WT 50 LBS, Manufactured By: Newly…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B82379, BATTER MIX, NET WT 50 LBS, Manufactured By: Newly We…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B81954, BATTER MIX, NET WT 50 LBS, Manufactured By: Newly We…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 5, 2019Historical recordClass II

Newly Weds Foods Inc

Product: B5Q68N, BREADER (1/25#) X1, NET WT 25 LBS, Manufactured By:…
Reason: Product may contain undeclared milk.
Published: July 26, 2017
Distribution: Nationwide

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Data last updated: November 9, 2026 ET

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.